Medline Epidural Catheter
Brand(s)
Last updated
Summary
Product
Medline Epidural Catheter
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Epidural Catheter | 23GBO701 23GBO702 23GBO700 22FBX111 23GBL403 23FBT886 22FBY472 | EPICATH19 |
Issue
Medline Industries, LP has initiated a recall on convenience kits containing NEXUS™ Connectors A-EP-081 and A-EP-424 from Epimed International Inc. The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position. If the defect is not detected before use, there is a risk of medication leakage. Additionally, if the defect goes unnoticed, there is a risk of the catheter connector disconnecting during use.
Recall start date: October 25, 2024
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Obstetrics and gynaecology
Companies
| Medline Industries, Lp |
| Three Lakes Drive, Northfield, Illinois, United States, 60093 |
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-76460
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